Fábrega María-José, Rodríguez-Nogales Alba, Garrido-Mesa José, Algieri Francesca, Badía Josefa, Giménez Rosa, Gálvez Julio, Baldomà Laura
Departament de Bioquímica i Fisiologia, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Institut de Biomedicina de la, Universitat de BarcelonaBarcelona, Spain.
Microbiota Intestinal, Institut de Recerca Sant Joan de DéuEsplugues de Llobregat, Spain.
Front Microbiol. 2017 Jul 11;8:1274. doi: 10.3389/fmicb.2017.01274. eCollection 2017.
Nissle 1917 (EcN) is a probiotic strain with proven efficacy in inducing and maintaining remission of ulcerative colitis. However, the microbial factors that mediate these beneficial effects are not fully known. Gram-negative bacteria release outer membrane vesicles (OMVs) as a direct pathway for delivering selected bacterial proteins and active compounds to the host. In fact, vesicles released by gut microbiota are emerging as key players in signaling processes in the intestinal mucosa. In the present study, the dextran sodium sulfate (DSS)-induced colitis mouse model was used to investigate the potential of EcN OMVs to ameliorate mucosal injury and inflammation in the gut. The experimental protocol involved pre-treatment with OMVs for 10 days before DSS intake, and a 5-day recovery period. Oral administration of purified EcN OMVs (5 μg/day) significantly reduced DSS-induced weight loss and ameliorated clinical symptoms and histological scores. OMVs treatment counteracted altered expression of cytokines and markers of intestinal barrier function. This study shows for the first time that EcN OMVs can mediate the anti-inflammatory and barrier protection effects previously reported for this probiotic in experimental colitis. Remarkably, translation of probiotics to human healthcare requires knowledge of the molecular mechanisms involved in probiotic-host interactions. Thus, OMVs, as a non-replicative bacterial form, could be explored as a new probiotic-derived therapeutic approach, with even lower risk of adverse events than probiotic administration.
Nissle 1917(大肠杆菌Nissle 1917)是一种益生菌菌株,在诱导和维持溃疡性结肠炎缓解方面具有已证实的疗效。然而,介导这些有益作用的微生物因素尚不完全清楚。革兰氏阴性菌释放外膜囊泡(OMVs),作为将特定细菌蛋白和活性化合物递送至宿主的直接途径。事实上,肠道微生物群释放的囊泡正成为肠黏膜信号传导过程中的关键参与者。在本研究中,使用葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠模型来研究大肠杆菌Nissle 1917外膜囊泡改善肠道黏膜损伤和炎症的潜力。实验方案包括在摄入DSS前用外膜囊泡预处理10天,以及5天的恢复期。口服纯化的大肠杆菌Nissle 1917外膜囊泡(5微克/天)显著减轻了DSS诱导的体重减轻,并改善了临床症状和组织学评分。外膜囊泡治疗抵消了细胞因子表达的改变和肠道屏障功能标志物的变化。本研究首次表明,大肠杆菌Nissle 1917外膜囊泡可以介导先前报道的该益生菌在实验性结肠炎中的抗炎和屏障保护作用。值得注意的是,将益生菌应用于人类医疗保健需要了解益生菌与宿主相互作用所涉及的分子机制。因此,外膜囊泡作为一种非复制性细菌形式,可以作为一种新的益生菌衍生治疗方法进行探索,其不良事件风险甚至低于益生菌给药。